JPH0470356B2 - - Google Patents
Info
- Publication number
- JPH0470356B2 JPH0470356B2 JP62162966A JP16296687A JPH0470356B2 JP H0470356 B2 JPH0470356 B2 JP H0470356B2 JP 62162966 A JP62162966 A JP 62162966A JP 16296687 A JP16296687 A JP 16296687A JP H0470356 B2 JPH0470356 B2 JP H0470356B2
- Authority
- JP
- Japan
- Prior art keywords
- volume
- component
- methyl
- gasoline
- dimethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 23
- 150000002430 hydrocarbons Chemical class 0.000 claims description 22
- 239000004215 Carbon black (E152) Substances 0.000 claims description 15
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 8
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 230000001133 acceleration Effects 0.000 description 16
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 description 4
- WGECXQBGLLYSFP-UHFFFAOYSA-N 2,3-dimethylpentane Chemical compound CCC(C)C(C)C WGECXQBGLLYSFP-UHFFFAOYSA-N 0.000 description 4
- -1 3-methyl-4-ethylhexane 2,2,3 -trimethylhexane Chemical compound 0.000 description 4
- 230000009194 climbing Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- BZHMBWZPUJHVEE-UHFFFAOYSA-N 2,3-dimethylpentane Natural products CC(C)CC(C)C BZHMBWZPUJHVEE-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- PLZDDPSCZHRBOY-UHFFFAOYSA-N inaktives 3-Methyl-nonan Natural products CCCCCCC(C)CC PLZDDPSCZHRBOY-UHFFFAOYSA-N 0.000 description 3
- 239000001282 iso-butane Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- IQANHWBWTVLDTP-AATRIKPKSA-N (e)-2-methylhex-3-ene Chemical compound CC\C=C\C(C)C IQANHWBWTVLDTP-AATRIKPKSA-N 0.000 description 2
- BFIMMTCNYPIMRN-UHFFFAOYSA-N 1,2,3,5-tetramethylbenzene Chemical compound CC1=CC(C)=C(C)C(C)=C1 BFIMMTCNYPIMRN-UHFFFAOYSA-N 0.000 description 2
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LETYIFNDQBJGPJ-UHFFFAOYSA-N 1-ethyl-1-methylcyclopentane Chemical compound CCC1(C)CCCC1 LETYIFNDQBJGPJ-UHFFFAOYSA-N 0.000 description 2
- QUBBAXISAHIDNM-UHFFFAOYSA-N 1-ethyl-2,3-dimethylbenzene Chemical compound CCC1=CC=CC(C)=C1C QUBBAXISAHIDNM-UHFFFAOYSA-N 0.000 description 2
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- GCFKTDRTZYDRBI-UHFFFAOYSA-N 2,2,3,5-tetramethylhexane Chemical compound CC(C)CC(C)C(C)(C)C GCFKTDRTZYDRBI-UHFFFAOYSA-N 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- FLTJDUOFAQWHDF-UHFFFAOYSA-N 2,2-dimethylhexane Chemical compound CCCCC(C)(C)C FLTJDUOFAQWHDF-UHFFFAOYSA-N 0.000 description 2
- CXOWYJMDMMMMJO-UHFFFAOYSA-N 2,2-dimethylpentane Chemical compound CCCC(C)(C)C CXOWYJMDMMMMJO-UHFFFAOYSA-N 0.000 description 2
- RUTNOQHQISEBGT-UHFFFAOYSA-N 2,3,4-trimethylhexane Chemical compound CCC(C)C(C)C(C)C RUTNOQHQISEBGT-UHFFFAOYSA-N 0.000 description 2
- ODGLTLJZCVNPBU-UHFFFAOYSA-N 2,3,5-trimethylhexane Chemical compound CC(C)CC(C)C(C)C ODGLTLJZCVNPBU-UHFFFAOYSA-N 0.000 description 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical compound CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
- WBRFDUJXCLCKPX-UHFFFAOYSA-N 2,3-dimethylheptane Chemical compound CCCCC(C)C(C)C WBRFDUJXCLCKPX-UHFFFAOYSA-N 0.000 description 2
- HDGQICNBXPAKLR-UHFFFAOYSA-N 2,4-dimethylhexane Chemical compound CCC(C)CC(C)C HDGQICNBXPAKLR-UHFFFAOYSA-N 0.000 description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical compound CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- KBPCCVWUMVGXGF-UHFFFAOYSA-N 2,6-dimethylheptane Chemical compound CC(C)CCCC(C)C KBPCCVWUMVGXGF-UHFFFAOYSA-N 0.000 description 2
- ZALHPSXXQIPKTQ-UHFFFAOYSA-N 2,6-dimethyloctane Chemical compound CCC(C)CCCC(C)C ZALHPSXXQIPKTQ-UHFFFAOYSA-N 0.000 description 2
- KEVMYFLMMDUPJE-UHFFFAOYSA-N 2,7-dimethyloctane Chemical compound CC(C)CCCCC(C)C KEVMYFLMMDUPJE-UHFFFAOYSA-N 0.000 description 2
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N 2-Methylheptane Chemical compound CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methyl-1-pentene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-UHFFFAOYSA-N 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 2
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Chemical compound CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 2
- SGVYKUFIHHTIFL-UHFFFAOYSA-N 2-methylnonane Chemical compound CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 2
- JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical compound CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 description 2
- RXYYKIMRVXDSFR-UHFFFAOYSA-N 3,3-dimethylhex-1-ene Chemical compound CCCC(C)(C)C=C RXYYKIMRVXDSFR-UHFFFAOYSA-N 0.000 description 2
- AEXMKKGTQYQZCS-UHFFFAOYSA-N 3,3-dimethylpentane Chemical compound CCC(C)(C)CC AEXMKKGTQYQZCS-UHFFFAOYSA-N 0.000 description 2
- MAKRYGRRIKSDES-UHFFFAOYSA-N 3,4-dimethylheptane Chemical compound CCCC(C)C(C)CC MAKRYGRRIKSDES-UHFFFAOYSA-N 0.000 description 2
- DZJTZGHZAWTWGA-UHFFFAOYSA-N 3,5-dimethylheptane Chemical compound CCC(C)CC(C)CC DZJTZGHZAWTWGA-UHFFFAOYSA-N 0.000 description 2
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
- DUPUVYJQZSLSJB-UHFFFAOYSA-N 3-ethyl-2-methylpentane Chemical compound CCC(CC)C(C)C DUPUVYJQZSLSJB-UHFFFAOYSA-N 0.000 description 2
- CYWROHZCELEGSE-UHFFFAOYSA-N 3-ethyl-3-methylhexane Chemical compound CCCC(C)(CC)CC CYWROHZCELEGSE-UHFFFAOYSA-N 0.000 description 2
- SFRKSDZMZHIISH-UHFFFAOYSA-N 3-ethylhexane Chemical compound CCCC(CC)CC SFRKSDZMZHIISH-UHFFFAOYSA-N 0.000 description 2
- XMYFZAWUNVHVGI-UHFFFAOYSA-N 3-ethylpent-2-ene Chemical compound CCC(CC)=CC XMYFZAWUNVHVGI-UHFFFAOYSA-N 0.000 description 2
- AORMDLNPRGXHHL-UHFFFAOYSA-N 3-ethylpentane Chemical compound CCC(CC)CC AORMDLNPRGXHHL-UHFFFAOYSA-N 0.000 description 2
- VLJXXKKOSFGPHI-UHFFFAOYSA-N 3-methylhexane Chemical compound CCCC(C)CC VLJXXKKOSFGPHI-UHFFFAOYSA-N 0.000 description 2
- SEEOMASXHIJCDV-UHFFFAOYSA-N 3-methyloctane Chemical compound CCCCCC(C)CC SEEOMASXHIJCDV-UHFFFAOYSA-N 0.000 description 2
- PFEOZHBOMNWTJB-UHFFFAOYSA-N 3-methylpentane Chemical compound CCC(C)CC PFEOZHBOMNWTJB-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- CHBAWFGIXDBEBT-UHFFFAOYSA-N 4-methylheptane Chemical compound CCCC(C)CCC CHBAWFGIXDBEBT-UHFFFAOYSA-N 0.000 description 2
- DOGIHOCMZJUJNR-UHFFFAOYSA-N 4-methyloctane Chemical compound CCCCC(C)CCC DOGIHOCMZJUJNR-UHFFFAOYSA-N 0.000 description 2
- DFVOXRAAHOJJBN-UHFFFAOYSA-N 6-methylhept-1-ene Chemical compound CC(C)CCCC=C DFVOXRAAHOJJBN-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- IFTRQJLVEBNKJK-UHFFFAOYSA-N Ethylcyclopentane Chemical compound CCC1CCCC1 IFTRQJLVEBNKJK-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- PWATWSYOIIXYMA-UHFFFAOYSA-N Pentylbenzene Chemical compound CCCCCC1=CC=CC=C1 PWATWSYOIIXYMA-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 2
- 238000004523 catalytic cracking Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 239000003747 fuel oil additive Substances 0.000 description 2
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 2
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 2
- KDIAMAVWIJYWHN-UHFFFAOYSA-N propylcyclopentane Chemical compound CCCC1CCCC1 KDIAMAVWIJYWHN-UHFFFAOYSA-N 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- ZISSAWUMDACLOM-UHFFFAOYSA-N triptane Chemical compound CC(C)C(C)(C)C ZISSAWUMDACLOM-UHFFFAOYSA-N 0.000 description 2
- JXPOLSKBTUYKJB-UHFFFAOYSA-N xi-2,3-Dimethylhexane Chemical compound CCCC(C)C(C)C JXPOLSKBTUYKJB-UHFFFAOYSA-N 0.000 description 2
- PBWHJRFXUPLZDS-UHFFFAOYSA-N (1-Ethylpropyl)benzene Chemical compound CCC(CC)C1=CC=CC=C1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 description 1
- BIDIHFPLDRSAMB-AATRIKPKSA-N (E)-4,4-Dimethyl-2-pentene Chemical compound C\C=C\C(C)(C)C BIDIHFPLDRSAMB-AATRIKPKSA-N 0.000 description 1
- OTTZHAVKAVGASB-HWKANZROSA-N (E)-Hept-2-ene Chemical compound CCCC\C=C\C OTTZHAVKAVGASB-HWKANZROSA-N 0.000 description 1
- JPLZSSHKQZJYTJ-VOTSOKGWSA-N (e)-2,2-dimethylhex-3-ene Chemical compound CC\C=C\C(C)(C)C JPLZSSHKQZJYTJ-VOTSOKGWSA-N 0.000 description 1
- KNCMKWVOMRUHKZ-AATRIKPKSA-N (e)-2,5-dimethylhex-3-ene Chemical compound CC(C)\C=C\C(C)C KNCMKWVOMRUHKZ-AATRIKPKSA-N 0.000 description 1
- PPBWEVVDSRKEIK-FNORWQNLSA-N (e)-3,4-dimethylpent-2-ene Chemical compound C\C=C(/C)C(C)C PPBWEVVDSRKEIK-FNORWQNLSA-N 0.000 description 1
- OQEVAISXHCRQGF-FNORWQNLSA-N (e)-4,4-dimethylhex-2-ene Chemical compound CCC(C)(C)\C=C\C OQEVAISXHCRQGF-FNORWQNLSA-N 0.000 description 1
- OAVNNZUEVHDCKP-AATRIKPKSA-N (e)-4,5-dimethylhex-2-ene Chemical compound C\C=C\C(C)C(C)C OAVNNZUEVHDCKP-AATRIKPKSA-N 0.000 description 1
- MBNDKEPQUVZHCM-GQCTYLIASA-N (e)-4-methylhex-2-ene Chemical compound CCC(C)\C=C\C MBNDKEPQUVZHCM-GQCTYLIASA-N 0.000 description 1
- NWZJLSKAFZXSQH-AATRIKPKSA-N (e)-5,5-dimethylhex-2-ene Chemical compound C\C=C\CC(C)(C)C NWZJLSKAFZXSQH-AATRIKPKSA-N 0.000 description 1
- GHBKCPRDHLITSE-SNAWJCMRSA-N (e)-5-methylhex-2-ene Chemical compound C\C=C\CC(C)C GHBKCPRDHLITSE-SNAWJCMRSA-N 0.000 description 1
- GVRWIAHBVAYKIZ-FNORWQNLSA-N (e)-dec-3-ene Chemical compound CCCCCC\C=C\CC GVRWIAHBVAYKIZ-FNORWQNLSA-N 0.000 description 1
- IICQZTQZQSBHBY-HWKANZROSA-N (e)-non-2-ene Chemical compound CCCCCC\C=C\C IICQZTQZQSBHBY-HWKANZROSA-N 0.000 description 1
- YCBSHDKATAPNIA-FNORWQNLSA-N (e)-non-3-ene Chemical compound CCCCC\C=C\CC YCBSHDKATAPNIA-FNORWQNLSA-N 0.000 description 1
- JPLZSSHKQZJYTJ-SREVYHEPSA-N (z)-2,2-dimethylhex-3-ene Chemical compound CC\C=C/C(C)(C)C JPLZSSHKQZJYTJ-SREVYHEPSA-N 0.000 description 1
- VFCHHMABGOYOQI-VURMDHGXSA-N (z)-2,4-dimethylhex-3-ene Chemical compound CC\C(C)=C/C(C)C VFCHHMABGOYOQI-VURMDHGXSA-N 0.000 description 1
- KNCMKWVOMRUHKZ-WAYWQWQTSA-N (z)-2,5-dimethylhex-3-ene Chemical compound CC(C)\C=C/C(C)C KNCMKWVOMRUHKZ-WAYWQWQTSA-N 0.000 description 1
- IQANHWBWTVLDTP-WAYWQWQTSA-N (z)-2-methylhex-3-ene Chemical compound CC\C=C/C(C)C IQANHWBWTVLDTP-WAYWQWQTSA-N 0.000 description 1
- PPBWEVVDSRKEIK-ALCCZGGFSA-N (z)-3,4-dimethylpent-2-ene Chemical compound C\C=C(\C)C(C)C PPBWEVVDSRKEIK-ALCCZGGFSA-N 0.000 description 1
- JZMUUSXQSKCZNO-ALCCZGGFSA-N (z)-3-methylhex-2-ene Chemical compound CCC\C(C)=C/C JZMUUSXQSKCZNO-ALCCZGGFSA-N 0.000 description 1
- FHHSSXNRVNXTBG-SREVYHEPSA-N (z)-3-methylhex-3-ene Chemical compound CC\C=C(\C)CC FHHSSXNRVNXTBG-SREVYHEPSA-N 0.000 description 1
- MBNDKEPQUVZHCM-XQRVVYSFSA-N (z)-4-methylhex-2-ene Chemical compound CCC(C)\C=C/C MBNDKEPQUVZHCM-XQRVVYSFSA-N 0.000 description 1
- LGAQJENWWYGFSN-PLNGDYQASA-N (z)-4-methylpent-2-ene Chemical compound C\C=C/C(C)C LGAQJENWWYGFSN-PLNGDYQASA-N 0.000 description 1
- NWZJLSKAFZXSQH-WAYWQWQTSA-N (z)-5,5-dimethylhex-2-ene Chemical compound C\C=C/CC(C)(C)C NWZJLSKAFZXSQH-WAYWQWQTSA-N 0.000 description 1
- GHBKCPRDHLITSE-PLNGDYQASA-N (z)-5-methylhex-2-ene Chemical compound C\C=C/CC(C)C GHBKCPRDHLITSE-PLNGDYQASA-N 0.000 description 1
- UURSXESKOOOTOV-KTKRTIGZSA-N (z)-dec-5-ene Chemical compound CCCC\C=C/CCCC UURSXESKOOOTOV-KTKRTIGZSA-N 0.000 description 1
- WZHKDGJSXCTSCK-ALCCZGGFSA-N (z)-hept-3-ene Chemical compound CCC\C=C/CC WZHKDGJSXCTSCK-ALCCZGGFSA-N 0.000 description 1
- IICQZTQZQSBHBY-HYXAFXHYSA-N (z)-non-2-ene Chemical compound CCCCCC\C=C/C IICQZTQZQSBHBY-HYXAFXHYSA-N 0.000 description 1
- YCBSHDKATAPNIA-ALCCZGGFSA-N (z)-non-3-ene Chemical compound CCCCC\C=C/CC YCBSHDKATAPNIA-ALCCZGGFSA-N 0.000 description 1
- KPADFPAILITQBG-CLFYSBASSA-N (z)-non-4-ene Chemical compound CCCC\C=C/CCC KPADFPAILITQBG-CLFYSBASSA-N 0.000 description 1
- WINCSBAYCULVDU-UHFFFAOYSA-N 1,1,2-trimethylcyclopentane Chemical compound CC1CCCC1(C)C WINCSBAYCULVDU-UHFFFAOYSA-N 0.000 description 1
- FAWZMJHFENIDPI-UHFFFAOYSA-N 1,2-diethyl-3,4-dimethylbenzene Chemical compound CCC1=CC=C(C)C(C)=C1CC FAWZMJHFENIDPI-UHFFFAOYSA-N 0.000 description 1
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- DOYJTLUPPPUSMD-UHFFFAOYSA-N 4,5-dimethyloctane Chemical compound CCCC(C)C(C)CCC DOYJTLUPPPUSMD-UHFFFAOYSA-N 0.000 description 1
- IALRSQMWHFKJJA-UHFFFAOYSA-N 4-Methylnonane Natural products CCCCCC(C)CCC IALRSQMWHFKJJA-UHFFFAOYSA-N 0.000 description 1
- JABYJIQOLGWMQW-VQHVLOKHSA-N 4-Undecene Chemical compound CCCCCC\C=C\CCC JABYJIQOLGWMQW-VQHVLOKHSA-N 0.000 description 1
- QHLDBFLIDFTHQI-UHFFFAOYSA-N 4-ethyl-2,2-dimethylhexane Chemical compound CCC(CC)CC(C)(C)C QHLDBFLIDFTHQI-UHFFFAOYSA-N 0.000 description 1
- RHMRCCBCYFAZIK-UHFFFAOYSA-N 4-ethyl-2,3-dimethylhexane Chemical compound CCC(CC)C(C)C(C)C RHMRCCBCYFAZIK-UHFFFAOYSA-N 0.000 description 1
- SIKFMUYSQCEQOO-UHFFFAOYSA-N 4-ethyl-2,4-dimethylhexane Chemical compound CCC(C)(CC)CC(C)C SIKFMUYSQCEQOO-UHFFFAOYSA-N 0.000 description 1
- OJDKRASKNKPYDH-UHFFFAOYSA-N 4-ethyl-2-methylheptane Chemical compound CCCC(CC)CC(C)C OJDKRASKNKPYDH-UHFFFAOYSA-N 0.000 description 1
- KYCZJIBOPKRSOV-UHFFFAOYSA-N 4-ethyl-2-methylhexane Chemical compound CCC(CC)CC(C)C KYCZJIBOPKRSOV-UHFFFAOYSA-N 0.000 description 1
- ZRTXVJYJVBTXHE-UHFFFAOYSA-N 4-ethyl-3,3-dimethylhexane Chemical compound CCC(CC)C(C)(C)CC ZRTXVJYJVBTXHE-UHFFFAOYSA-N 0.000 description 1
- BTGGSWBKRYMHQK-UHFFFAOYSA-N 4-ethyl-3-methylheptane Chemical compound CCCC(CC)C(C)CC BTGGSWBKRYMHQK-UHFFFAOYSA-N 0.000 description 1
- MPYQJQDSICRCJJ-UHFFFAOYSA-N 4-ethyl-4-methylheptane Chemical compound CCCC(C)(CC)CCC MPYQJQDSICRCJJ-UHFFFAOYSA-N 0.000 description 1
- XMROPFQWHHUFFS-UHFFFAOYSA-N 4-ethylheptane Chemical compound CCCC(CC)CCC XMROPFQWHHUFFS-UHFFFAOYSA-N 0.000 description 1
- NRJUFUBKIFIKFI-UHFFFAOYSA-N 4-ethyloctane Chemical compound CCCCC(CC)CCC NRJUFUBKIFIKFI-UHFFFAOYSA-N 0.000 description 1
- SUWJESCICIOQHO-UHFFFAOYSA-N 4-methylhex-1-ene Chemical compound CCC(C)CC=C SUWJESCICIOQHO-UHFFFAOYSA-N 0.000 description 1
- AZLAWGCUDHUQDB-UHFFFAOYSA-N 4-propan-2-ylheptane Chemical compound CCCC(C(C)C)CCC AZLAWGCUDHUQDB-UHFFFAOYSA-N 0.000 description 1
- ABYGSZMCWVXFCQ-UHFFFAOYSA-N 4-propylheptane Chemical compound CCCC(CCC)CCC ABYGSZMCWVXFCQ-UHFFFAOYSA-N 0.000 description 1
- KZJIOVQKSAOPOP-UHFFFAOYSA-N 5,5-dimethylhex-1-ene Chemical compound CC(C)(C)CCC=C KZJIOVQKSAOPOP-UHFFFAOYSA-N 0.000 description 1
- DGEMPTLPTFNEHJ-UHFFFAOYSA-N 5-ethyl-2-methylheptane Chemical compound CCC(CC)CCC(C)C DGEMPTLPTFNEHJ-UHFFFAOYSA-N 0.000 description 1
- JIUFYGIESXPUPL-UHFFFAOYSA-N 5-methylhex-1-ene Chemical compound CC(C)CCC=C JIUFYGIESXPUPL-UHFFFAOYSA-N 0.000 description 1
- TYSIILFJZXHVPU-UHFFFAOYSA-N 5-methylnonane Chemical compound CCCCC(C)CCCC TYSIILFJZXHVPU-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- IALRSQMWHFKJJA-JTQLQIEISA-N Nonane, 4-methyl- Chemical compound CCCCC[C@@H](C)CCC IALRSQMWHFKJJA-JTQLQIEISA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- ZAGHKONXGGSVDV-UHFFFAOYSA-N butylcyclopentane Chemical compound CCCCC1CCCC1 ZAGHKONXGGSVDV-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000001833 catalytic reforming Methods 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- UURSXESKOOOTOV-UHFFFAOYSA-N dec-5-ene Chemical compound CCCCC=CCCCC UURSXESKOOOTOV-UHFFFAOYSA-N 0.000 description 1
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 1
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003269 fluorescent indicator Substances 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- IRUCBBFNLDIMIK-UHFFFAOYSA-N oct-4-ene Chemical compound CCCC=CCCC IRUCBBFNLDIMIK-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- QRMPKOFEUHIBNM-UHFFFAOYSA-N p-dimethylcyclohexane Natural products CC1CCC(C)CC1 QRMPKOFEUHIBNM-UHFFFAOYSA-N 0.000 description 1
- LTHAIAJHDPJXLG-UHFFFAOYSA-N pentan-2-ylbenzene Chemical compound CCCC(C)C1=CC=CC=C1 LTHAIAJHDPJXLG-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- ZJMWRROPUADPEA-UHFFFAOYSA-N sec-butylbenzene Chemical compound CCC(C)C1=CC=CC=C1 ZJMWRROPUADPEA-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Liquid Carbonaceous Fuels (AREA)
Description
産業上の利用分野
本発明は無鉛ガソリンに関し、詳しくは特定さ
れた成分組成を有する、各種性能に優れた無鉛ガ
ソリンに関する。
従来の技術および発明が解決しようとする問題点
我国では昭和50年よりオクタン価90〜91の無鉛
レギユラーガソリンが市販され、また昭和59年に
は運転条件によつてノツキングを起こしやすいと
いう無鉛レギユラーガソリンの持つ欠点を克服し
た、96〜98という高いオクタン価を有する無鉛高
オクタン価ガソリンが発売された。無鉛高オクタ
ン価ガソリンの出現によりノツキングの問題は一
応解消されたものの、最近の自動車技術の向上に
伴い、レギユラーガソリンおよび高オクタン価ガ
ソリンともより高度の運転性を可能にする品質を
有するもの、すなわち始動性に優れ、低速域、中
速域、高速域ならびに登坂時の加速性に優れ、さ
らに走行安定性の優れた新しいタイプの無鉛ガソ
リンの出現が要望されるようになつてきた。
そこで本発明者らは上記の要求を満足する新ガ
ソリンを開発すべく研究を重ねた結果、その成分
組成を細かく規定することにより、極めて優れた
性能を有する新しいタイプの無鉛ガソリンが得ら
れることを見い出し、本発明を完成するに至つ
た。
本発明は、従来の無鉛ガソリンと比べて、停止
状態から低速への加速、低速から中速への加速、
中速から高速への加速、高速でのさらなる加速
性、登坂力などの各種加速性、低温での始動性お
よび低温での運転性(暖機性)がさらに向上し
た、新規な無鉛ガソリンを提供することを目的と
する。
問題点を解決するための手段
すなわち、本発明は、
(a) 炭素数4〜6のパラフイン系炭化水素15〜30
容量%、
(b) 炭素数7〜8のパラフイン系炭化水素10〜25
容量%、
(c) 炭素数9〜11のパラフイン系炭化水素1〜8
容量%、
(d) 炭素数4〜6のオレフイン系炭化水素0〜25
容量%、
(e) 炭素数7〜8のオレフイン系炭化水素0〜7
容量%、
(f) 炭素数9〜11のオレフイン系炭化水素0〜5
容量%、
(g) 炭素数6〜7の芳香族系炭化水素3〜8容量
%、
および
(h) 炭素数8〜12の芳香族系炭化水素15〜40容量
%
を必須成分として含有し、かつ以下の(1)〜(5)式の
条件を満たす成分組成を有することを特徴とする
無鉛ガソリン。
35≦(a)+(d)≦45(容量%) (1)
15≦(b)+(e)+(g)≦30(容量%) (2)
35≦(c)+(f)+(h)≦45(容量%) (3)
0≦VO(WHOLE)≦25(容量%) (4)
VA(WHOLE)≦50(容量%) (5)
を提供するものである。なお上式中で、(a)+(d)は
(a)成分および(d)成分、(b)+(e)+(g)は(b)成分、(e)
成
分および(g)成分ならびに(c)+(f)+(h)は(c)成分、(f)
成分および(h)成分の合計量(容量%)をそれぞれ
示し、またVO(WHOLE)およびVA(WHOLE)
はガソリン全体のオレフイン分および芳香族分含
量(容量%)をそれぞれ示している。
以下、本発明の内容をさらに詳細に説明する。
本発明における(a)成分とは炭素数4〜6のパラ
フイン系炭化水素であり、具体的には例えば、n
−ブタン、イソブタン、n−ペンタン、イソペン
タン、ネオペンタン、n−ヘキサン、2−メチル
ペンタン、3−メチルペンタン、2,2−ジメチ
ルブタン、2,3−ジメチルブタンまたはこれら
の中から選ばれる2種類以上の化合物の混合物な
どが挙げられる。(a)成分のガソリン全体に対する
含有量は15〜30容量%、好ましくは17〜25容量%
である。
本発明における(b)成分とは、炭素数7〜8のパ
ラフイン系炭化水素であり、具体的には例えば、
n−ヘプタン、2−メチルヘキサン、3−メチル
ヘキサン、2,2−ジメチルペンタン、2,3−
ジメチルペンタン、2,4−ジメチルペンタン、
3,3−ジメチルペンタン、3−エチルペンタ
ン、2,2,3−トリメチエルブタン、n−オク
タン、2−メチルヘプタン、3−メチルヘプタ
ン、4−メチルヘプタン、2,2−ジメチルヘキ
サン、2,3−ジメチルヘキサン、2,4−ジメ
チルヘキサン、2,5−ジメチルヘキサン、3−
エチルヘキサン、2,2,3−トリメチルペンタ
ン、2,2,4−トリメチルペンタン、2,3,
3−トリメチルペンタン、2,3,4−トリメチ
ルペンタン、2−メチル−3−エチルペンタン、
3−メチル−3−エチルペンタン、2,2,3,
3−テトラメチルブタン、またはこれらの中より
選ばれる2種類以上の化合物の混合物などが挙げ
られる。(b)成分のガソリン全体に対する含有量は
10〜25容量%、好ましくは12〜20容量%である。
本発明における(c)成分とは、炭素数9〜11のパ
ラフイン系炭化水素であり、具体的には例えば、
n−ノナン、2−メチルオクタン、3−メチルオ
クタン、4−メチルオクタン、2,2−ジメチル
ヘプタン、2,3−ジメチルヘプタン、2,4−
ジメチルヘプタン、2,5−ジメチルヘプタン、
2,6−ジメチルヘプタン、3,3−ジメチルヘ
プタン、3,4−ジメチルヘプタン、3,5−ジ
メチルヘプタン、4,4−ジメチルヘプタン、3
−エチルヘプタン、4−エチルヘプタン、2−メ
チル−3−エチルヘキサン、2−メチル−4−エ
チルヘキサン、3−メチル−3−エチルヘキサ
ン、3−メチル−4−エチルヘキサン2,2,3
−トリメチルヘキサン、2,2,4−トリメチル
ヘキサン、2,2,5−トリメチルヘキサン、
2,3,3−トリメチルヘキサン、2,3,4−
トリメチルヘキサン、2,3,5−トリメチルヘ
キサン、2,4,4−トリメチルヘキサン、3,
3,4−トリメチルヘキサン、2,2,3,3−
テトラメチルペンタン、2,2,3,4−テトラ
メチルペンタン、2,2,4,4−テトラメチル
ペンタン、2,3,3,4−テトラメチルペンタ
ン、2,2−ジメチル−3−エチルペンタン、
2,3−ジメチル−3−エチルペンタン、2,4
−ジメチル−3−エチルペンタン、n−デカン、
2,2,4,4−テトラメチルヘキサン、2,
2,5−トリメチルヘプタン、2,2,4,5−
テトラメチルヘキサン、2,2,6−トリメチル
ヘプタン、2,2,3,5−テトラメチルヘキサ
ン、2,2−ジメチル−4−エチルヘキサン、
2,2,4−トリメチルヘプタン、2,4−ジメ
チルオクタン、2,4,4−トリメチルヘプタ
ン、2,5,5−トリメチルヘプタン、2,2,
3,5−テトラメチルヘキサン、2,2,3,4
−テトラメチルヘキサン、2,2−ジメチルオク
タン、2,3,6−トリメチルヘプタン、3,
3,5−トリメチルヘプタン、2,4−ジメチル
−3−イソプロピルペンタン、2,3,5−トリ
メチルヘプタン、2,4,5−トリメチルヘプタ
ン、2,5−ジメチル−3−エチルヘキサン、
2,2,4−トリメチル−3−エチルペンタン、
2,5−ジメチルオクタン、2,2,3−トリメ
チルヘプタン、2,4−ジメチル−4−エチルヘ
キサン、2,6−ジメチルオクタン、2,2−ジ
メチル−3−エチルヘキサン、2,2,3,4,
4−ペンタメチルペンタン、2−メチル−5−エ
チルヘプタン、2,7−ジメチルオクタン、3,
5−ジメチルオクタン、3,6−ジメチルオクタ
ン、4−イソプロピルヘプタン、2−メチル−4
−エチルヘプタン、2,3,3−トリメチルヘプ
タン、2,2,3,3−テトラメチルヘキサン、
4,4−ジメチルオクタン、3−メチル−5−エ
チルヘプタン、2,3,4,5−テトラメチルヘ
キサン、3,3−ジメチルオクタン、4,5−ジ
メチルオクタン、4−プロピルヘプタン、3,4
−ジエチルヘキサン、2,3,4−トリメチルヘ
プタン、2−メチル−3−イソプロピルヘキサ
ン、2,3,4,4−テトラメチルヘキサン、
2,3−ジメチルオクタン、3−メチル−3−エ
チルヘプタン、3,3,4−トリメチルヘプタ
ン、3,4,4−トリメチルヘプタン、3,4,
5−トリメチルヘプタン、2,3−ジメチル−4
−エチルヘキサン、2,4−ジメチル−3−エチ
ルヘキサン、3,3−ジメチル−4−エチルヘキ
サン、5−メチルノナン、4−メチルノナン、
2,3,3,4−テトラメチルヘキサン、2,
2,3,3,4−ペンタメチルペンタン、3,4
−ジメチルオクタン、2−メチル−3−エチルヘ
プタン、3,3−ジエチルヘキサン、2−メチル
ノナン、3−メチル−4−エチルヘプタン、4−
メチル−3−エチルヘプタン、4−メチル−4−
エチルヘプタン、2,3,4−トリメチル−3−
エチルペンタン、3−エチルオクタン、4−エチ
ルオクタン、2,2,3−トリメチル−3−エチ
ルペンタン、3−メチルノナン、2,3−ジメチ
ル−3−エチルヘキサン、3,4−ジメチル−3
−エチルヘキサン、3,3,4,4−テトラメチ
ルヘキサン、2−メチル−3,3−ジエチルペン
タン、n−ウンデカンまたこれらの中より選ばれ
る2種類以上の化合物の混合物などが挙げられ
る。(c)成分のガソリン全体に対する含有量は1〜
8容量%、好ましくは1〜5容量%である。
本発明における(d)成分とは、炭素数4〜6のオ
レフイン系炭化水素であり、具体的には例えば、
1−ブテン、2−ブテン、イソブチレン、1−ペ
ンテン、2−ペンテン、2−メチル−1−ブテ
ン、3−メチル−1−ブテン、2−メチル−2−
ブテン、1−ヘキセン、2−ヘキセン、3−ヘキ
セン、2−メチル−1−ペンテン、3−メチル−
1−ペンテン、4−メチル−1−ペンテン、2−
メチル−2−ペンテン、3−メチル−2−ペンテ
ン、4−メチル−2−ペンテン、2−エチル−1
−ブテン、2,3−ジメチル−1−ブテン、2,
3−ジメチル−2−ブテンまたはこれらの中から
選ばれる2種類以上の化合物の混合物などが挙げ
られる。(d)成分のガソリン全体に対する含有量は
0〜25容量%、好ましくは0〜20容量%である。
本発明における(e)成分とは、炭素数7〜8のオ
レフイン系炭化水素であり、具体的には例えば、
4−4−ジメチル−1−ペンテン、シス−4,
4,ジメチル−2−ペンテン、トランス−4,4
−ジメチル−2−ペンテン、2,3,3−トリメ
チル−1−ブテン、2,4−ジメチル−1−ペン
テン、3,4−ジメチル−1−ペンテン、2,4
−ジメチル−2−ペンテン、3−メチル−1−ヘ
キセン、3−エチル−1−ペンテン、2,3−ジ
メチル−1−ペンテン、トランス−4−メチル−
2−ヘキセン、5−メチル−1−ヘキセン、トラ
ンス−5−メチル−2−ヘキセン、シス−2−メ
チル−3−ヘキセン、トランス−2−メチル−3
−ヘキセン、シス−3,4−ジメチル−2−ペン
テン、トランス−3,4−ジメチル−2−ペンテ
ン、4−メチル−1−ヘキセン、シス−4−メチ
ル−2−ヘキセン、3−メチル−2−エチル−1
−ブテン、シス−5−メチル−2−ヘキセン、2
−メチル−1−ヘキセン、1−ヘプテン、シス−
3−メチル−2−ヘキセン、トランス−3−メチ
ル−2−ヘキセン、シス−3−メチル−3−ヘキ
セン、トランス−3−メチル−3−ヘキセン、2
−エチル−1−ペンテン、3−エチル−2−ペン
テン、2−メチル−2−ヘキセン、シス−3−ヘ
プテン、トランス−3−ヘプテン2,3−ジメチ
ル−2−ペンテン、トランス−2−ヘプテン、シ
ス−2−ヘプテン、2,4,4−トリメチル−1
−ペンテン、5,5−ジメチル−1−ヘキセン、
シス−2,5−ジメチル−3−ヘキセン、トラン
ス−2,5−ジメチル−3−ヘキセン、3,4,
4−トリメチル−1−ペンテン、3−メチル−2
−イソプロピル−1−ブテン、3,3−ジメチル
−1−ヘキセン、3,5−ジメチル−1−ヘキセ
ン、2,4,4−トリメチル−2−ペンテン、
3,3,4−トリメチル−1−ペンテン、シス−
2,2−ジメチル−3−ヘキセン、トランス−
2,2−ジメチル−3−ヘキセン、シス−4,4
−ジメチル−2−ヘキセン、トランス−4,4−
ジメチル−2−ヘキセン、シス−5、5−ジメチ
ル−2−ヘキセン、トランス−5,5−ジメチル
−2−ヘキセン、4−メチル−3−エチル−1−
ペンテン、4,4−ジメチル−1−ヘキセン、シ
ス−2,4−ジメチル−3−ヘキセン、トランス
−2,4−ジメチル−3−ヘキセン、2,3,3
−トリメチル−1−ペンテン、2,3,4−トリ
メチル−1−ペンテン、4,5−ジメチル−1−
ヘキセン、2,4−ジメチル−2−ヘキセン、シ
ス−4,5−ジメチル−2−ヘキセン、トランス
−4,5−ジメチル−2−ヘキセン、2−メチル
−3−エチル−1−ペンテン、3,3−ジメチル
−2−エチル−1−ブテン、4−メチル−2−エ
チル−1−ペンタン、3−エチル−1−ヘキセ
ン、2,4−ジメチル−1−ヘキセン、2,5−
ジメチル−1−ヘキセン、3,3−ジメチルヘキ
セン、シス−3,5−ジメチル−2−ヘキセン、
3−メチル−3−エチル−1−ペンテン、3−メ
チル−2−エチル−1−ペンテン、6−メチル−
1−ヘプテン、3−エチル−3−ヘキセン、2−
メチル−2−ヘプテン、4−オクテンまたはこれ
らの中から選ばれる2種類以上の化合物の混合物
などが挙げられる。(e)成分のガソリン全体に対す
る含有量は0〜7容量%、好ましくは0〜5容量
%である。
本発明における(f)成分とは、炭素数9〜11のオ
レフイン系炭化水素であり、具体的には例えば、
1−ノネン、シス−2−ノネン、トランス−2−
ノネン、シス−3−ノネン、トランス−3−ノネ
ン、シス−4−ノネン、1−デセン、3−デセ
ン、1−ウンデセン、3−ウンデセン、トランス
−4−ウンデセン、シス−5−デセン、トランス
−5−デセンまたはこれらの中から選ばれる2種
類以上の化合物の混合物などが挙げられる。(f)成
分のガソリン全体に対する含有量は0〜5容量
%、好ましくは0〜4容量%である。
本発明における(g)成分とは、炭素数6〜7の芳
香族系炭化水素であり、具体的にはベンゼン、ト
ルエンおよびこれらの混合物が挙げられる。(g)成
分のガソリン全体に対する含有量は3〜8容量
%、好ましくは4〜7容量%である。
本発明における(h)成分とは、炭素数8〜12の芳
香族系炭化水素であり、具体的には例えば0−キ
シレン、m−キシレン、p−キシレン、エチルベ
ンゼン、n−プロピルベンゼン、イソプロピルベ
ンゼン、1−メチル−2−エチルベンゼン、トリ
メチルベンゼン、ブチルベンゼン、1−メチル−
プロピルベンゼン、ジエチルベンゼン、1,2−
ジメチル−3−エチルベンゼン、1,2,3,5
−テトラメチルベンゼン、2−フエニル−3−メ
チルブタン、3−フエニルペンタン、2−フエニ
ルペンタン、1−メチル−3−イソブチルベンゼ
ン、1−フエニル−2−メチルブタン、、1,3
−ジメチル−4−イソプロピルベンゼン、1−エ
チル−4−n−プロピルベンゼン、n−ペンチル
ベンゼン、1−メチル−4−n−ブチルベンゼ
ン、1−メチル−2,6−ジエチルベンゼン、
1,2,4−トリメチル−5−エチルベンゼン、
ジメチルジエチルベンゼンまたはこれらの中から
選ばれる2種類以上の化合物の混合物などが挙げ
られる。(h)成分のガソリン全体に対する含有量は
15〜40容量%、好ましくは25〜40容量%である。
本発明の無鉛ガソリンは上記(a)〜(h)成分を特定
量含有するだけでなく、さらに(1)〜(5)式の条件を
同時に満足する成分組成を有することが重要であ
る。
(1)式の条件は前記(a)成分と(d)成分の合計量が35
〜45容量%、好ましくは37〜45容量%であること
を、(2)式の条件は前記(b)成分、(e)成分および(g)成
分の合計量が15〜30容量%、好ましくは15〜27容
量%であることを、また(3)式の条件は前記(c)成
分、(f)成分および(h)成分の合計量が35〜45容量
%、好ましくは37〜45容量%であることをそれぞ
れ示している。本発明においてガソリンの成分組
成が(1)式、(2)式および(3)式の条件を同時に満足し
ない場合には、各種加速性および低温での始動性
や運転性(暖機性)が劣るため好ましくない。
一方、(4)式の条件はガソリン全体のオレフイン
分含量が0〜25容量%、好ましくは0〜20容量%
であることを、また(5)式はガソリン全体の芳香族
分含量が50容量%以下、好ましくは45容量%以下
であることをそれぞれ示している。なお、本発明
の(5)式および(6)式でいうオレフイン分含量および
芳香族分含量はJIS K 2536の燃料油炭化水素成
分試験方法(けい光指示薬吸着法)により測定さ
れる値を意味している。本発明において、ガソリ
ンの成分組成が(4)式および(5)式の条件を満足しな
い場合には、ガソリン自体の安定性が悪化した
り、自動車の排気ガスや燃料系統に使用されてい
る素材に対して悪影響を及ぼしたりする恐れがあ
るため好ましくない。
本発明の無鉛ガソリンを製造する際に用いる調
合材およびそれらの調合割合は任意であり、原油
の常圧蒸留により得られる直留ガソリン、原油の
常圧蒸留によるナフサ留分を分留して得られる軽
質ナフサ、接触分解法、水素化分解法などで得ら
れる分解ガソリン、接触改質法などで得られる改
質ガソリン、オレフインの重合により得られる重
合ガソリン、イソブタンなどの炭化水素に低級オ
レフインを付加(アルキル化)することにより得
られるアルキレート、直鎖の低級パラフイン系炭
化水素の異性化により得られるアイソメレート、
石油留分を分子ふるい法にかけて得られる脱n−
パラフイン油またはこれらの特定沸点範囲の留分
や芳香族炭化水素などを調合材として用いること
ができる。
しかしながら、本発明においては前述したとお
り、最終的に調合されたガソリンが(a)〜(h)成分を
特定量含有し、かつ(1)〜(5)式に示した成分組成の
条件を同時に満足することが重要であり、そのた
めには単に上記の調合材を混合すれば本発明の無
鉛ガソリンが製造できるというものではなく、使
用する調合材の組成および使用する調合材の組成
に応じた調合割合を厳密に選択する必要がある。
また本発明の無鉛ガソリンの組成については前
出の条件を満足することが重要であるが、その
他、JIS K 2254の燃料油蒸留試験方法で規定さ
れている10%留出温度が40〜55℃および90%留出
温度が150〜175℃の範囲内であることが望まし
い。また本発明の無鉛ガソリンはレギユラーガソ
リンとしても、高オクタン価ガソリンとしても使
用できる。レギユラーガソリンとして使用する場
合は95未満、好ましくは89以上95未満のリサーチ
法オクタン価を有することが、また高オクタン価
ガソリンとして使用する場合は95以上、好ましく
は98以上のリサーチ法オクタン価を有するもので
あることが望ましい。
本発明の無鉛ガソリンは前述の(a)〜(h)成分を特
定量含有するものであるが、その他炭素数5〜11
のナフテン系炭化水素、例えばシクロペンタン、
シクロヘキサン、メチルシクロペンタン、エチル
シクロペンタン、ジメチルシクロヘキサン、トリ
メチルシクロペンタン、メチルエチルシクロペン
タン、ジメチルシクロヘキサン、エチルシクロヘ
キサン、プロピルシクロペンタン、ブチルシクロ
ペンタンまたはこれらの中より選ばれる2種類以
上の化合物の混合物などを含有していてもよい。
これらナフテン系炭化水素の含有量は任意である
が、通常ガソリン全体に対して5容量%以下であ
る。
さらに、本発明の無鉛ガソリンにおいて、必要
に応じてフエノール系、アミン系などの酸化防止
剤、シツフ型化合物やチオアミド型化合物などの
金属不活性剤などの表面着火防止剤、こはく酸イ
ミド、ポリアルキルアミン、ポリエーテルアミン
などの清浄分散剤、多価アルコールおよびそのエ
ーテルなどの氷結防止剤、有機酸のアルカリ金属
やアルカリ土類金属塩、高級アルコールの硫酸エ
ステルなどの助燃剤、アニオン系界面活性剤、カ
チオン系界面活性剤、両性界面活性剤などの帯電
防止剤およびアゾ染料などの着色剤など、公知の
燃料油添加剤を1種または数種組み合わせて添加
してもよい。これら燃料油添加剤の添加量は任意
であるが、通常、その合計添加量が0.1重量%以
下となるように添加するのが好ましい。
またさらに、本発明の無鉛ガソリンに、必要に
応じてメタノール、エタノール、イソプロパノー
ル、t−ブタノールなどのアルコールやメチル−
t−ブチルエーテルなどのエーテルなどのオクタ
ン価向上剤を添加してもよい。これらオクタン価
向上剤の添加量も任意であるが、通常は15重量%
以下が好ましい。
実施例
以下、本発明の内容を実施例および比較例によ
りさらに具体的に説明する。
実施例および比較例
中東系原油より得られる接触改質ガソリン44容
量部、中東系原油より得られる流動接触分解ガソ
リンの軽質留分27容量部、中東系原油より得られ
る接触改質ガソリンの重質留分19容量部およびイ
ソブタンと低級オレフインのアルキル化反応によ
り得られたアルキレート10容量部を配合し、本発
明の無鉛ガソリンを得た。第1表に上記基材の組
成を、また第2表に得られた無鉛ガソリンの性状
および組成をそれぞれ示した。また比較のため、
市販の無鉛ガソリンの性状および組成を第2表に
示した。なお、第1表および第2表に示した組成
[VO(WHOLE)およびVA(WHOLE)を除く]
は、いずれもガスクロマトグラフイ・マススペク
トロメトリ(GCMS)分析によつて分離、固定
および定量したものである。
この実施例と比較例のガソリンを用いて以下に
示す各種の性能評価試験を行い、その結果を第3
表に示した。
[加速性能試験1(停止→低速、低速→中速、中
速→高速)]
総排気量1500c.c.、マニユアルトランスミツシヨ
ン、キヤブレター仕様の乗用自動車(A車)を使
用し、平坦路、絞り弁全開加速の条件でローギヤ
→セカンドギヤの順に変速して車速が0→60Km/
hr、ならびにトツプギヤで車速が40→80Km/hrお
よび80→120Km/hrに達するまでの時間を測定し
た。
[加速性能試験2 (登坂力)]
A車を使用し、5%上り勾配路、絞り弁全開加
速の条件でローギヤ→セカンドギヤの順に変速し
て車速が0→80Km/hr、およびサードギヤで車速
が40→80Km/hrに達するまでの時間を測定した。
[加速性能試験3 (登坂力)]
総排気量2000c.c.、オートマチツクトランスミツ
シヨン、燃料噴射式仕様の乗用自動車(B車)を
使用し、8%上り勾配路、絞り弁全開加速の条件
でDレンジで車速が0→120Km/hrに達するまで
の時間を測定した。
INDUSTRIAL APPLICATION FIELD The present invention relates to unleaded gasoline, and more particularly to unleaded gasoline having a specified component composition and excellent in various performances. Problems to be solved by conventional technology and inventions In Japan, unleaded regular gasoline with an octane number of 90 to 91 has been on the market since 1975, and in 1980, unleaded regular gasoline, which is prone to knocking depending on driving conditions, has been marketed. Unleaded high-octane gasoline with a high octane number of 96 to 98 has been released, overcoming the disadvantages of gasoline. Although the problem of knotting has been temporarily resolved with the advent of unleaded high octane gasoline, recent improvements in automobile technology have led to both regular gasoline and high octane gasoline having qualities that enable higher drivability. There has been a growing demand for a new type of unleaded gasoline that has excellent acceleration performance at low speeds, medium speeds, high speeds, and when climbing hills, as well as excellent running stability. As a result of repeated research to develop a new gasoline that satisfies the above requirements, the inventors of the present invention have found that by precisely specifying its component composition, a new type of unleaded gasoline with extremely superior performance can be obtained. This finding led to the completion of the present invention. Compared to conventional unleaded gasoline, the present invention improves acceleration from a standstill to low speeds, acceleration from low speeds to medium speeds,
Providing a new unleaded gasoline with improved acceleration from medium speeds to high speeds, further acceleration at high speeds, various types of acceleration such as hill-climbing power, and further improved startability at low temperatures and drivability (warm-up) at low temperatures. The purpose is to Means for Solving the Problems That is, the present invention provides (a) a paraffinic hydrocarbon having 4 to 6 carbon atoms, 15 to 30
Volume %, (b) Paraffinic hydrocarbons with 7 to 8 carbon atoms 10 to 25
Volume %, (c) Paraffinic hydrocarbons having 9 to 11 carbon atoms 1 to 8
Volume %, (d) Olefinic hydrocarbon having 4 to 6 carbon atoms 0 to 25
Volume %, (e) Olefinic hydrocarbon having 7 to 8 carbon atoms 0 to 7
Volume %, (f) Olefinic hydrocarbon having 9 to 11 carbon atoms 0 to 5
(g) 3 to 8 volume % of aromatic hydrocarbons having 6 to 7 carbon atoms, and (h) 15 to 40 volume % of aromatic hydrocarbons having 8 to 12 carbon atoms as essential components; An unleaded gasoline characterized by having a component composition that satisfies the conditions of formulas (1) to (5) below. 35≦(a)+(d)≦45 (capacity%) (1) 15≦(b)+(e)+(g)≦30 (capacity%) (2) 35≦(c)+(f)+ (h)≦45 (capacity%) (3) 0≦VO (WHOLE)≦25 (capacity%) (4) VA (WHOLE)≦50 (capacity%) (5). In the above formula, (a) + (d) is
(a) component and (d) component, (b) + (e) + (g) is (b) component, (e)
Component and (g) component and (c) + (f) + (h) are (c) component, (f)
Indicates the total amount (volume %) of component and (h) component, respectively, and also VO (WHOLE) and VA (WHOLE)
indicate the olefin content and aromatic content (volume %) of the entire gasoline, respectively. Hereinafter, the content of the present invention will be explained in more detail. Component (a) in the present invention is a paraffinic hydrocarbon having 4 to 6 carbon atoms, specifically, for example, n
-Butane, isobutane, n-pentane, isopentane, neopentane, n-hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, or two or more types selected from these and mixtures of these compounds. The content of component (a) in the entire gasoline is 15 to 30% by volume, preferably 17 to 25% by volume.
It is. Component (b) in the present invention is a paraffinic hydrocarbon having 7 to 8 carbon atoms, and specifically, for example,
n-heptane, 2-methylhexane, 3-methylhexane, 2,2-dimethylpentane, 2,3-
dimethylpentane, 2,4-dimethylpentane,
3,3-dimethylpentane, 3-ethylpentane, 2,2,3-trimethylbutane, n-octane, 2-methylheptane, 3-methylheptane, 4-methylheptane, 2,2-dimethylhexane, 2, 3-dimethylhexane, 2,4-dimethylhexane, 2,5-dimethylhexane, 3-
Ethylhexane, 2,2,3-trimethylpentane, 2,2,4-trimethylpentane, 2,3,
3-trimethylpentane, 2,3,4-trimethylpentane, 2-methyl-3-ethylpentane,
3-methyl-3-ethylpentane, 2,2,3,
Examples include 3-tetramethylbutane and a mixture of two or more compounds selected from these. The content of component (b) in the whole gasoline is
10-25% by volume, preferably 12-20% by volume. Component (c) in the present invention is a paraffinic hydrocarbon having 9 to 11 carbon atoms, and specifically, for example,
n-nonane, 2-methyloctane, 3-methyloctane, 4-methyloctane, 2,2-dimethylheptane, 2,3-dimethylheptane, 2,4-
dimethylheptane, 2,5-dimethylheptane,
2,6-dimethylheptane, 3,3-dimethylheptane, 3,4-dimethylheptane, 3,5-dimethylheptane, 4,4-dimethylheptane, 3
-Ethylheptane, 4-ethylheptane, 2-methyl-3-ethylhexane, 2-methyl-4-ethylhexane, 3-methyl-3-ethylhexane, 3-methyl-4-ethylhexane 2,2,3
-trimethylhexane, 2,2,4-trimethylhexane, 2,2,5-trimethylhexane,
2,3,3-trimethylhexane, 2,3,4-
Trimethylhexane, 2,3,5-trimethylhexane, 2,4,4-trimethylhexane, 3,
3,4-trimethylhexane, 2,2,3,3-
Tetramethylpentane, 2,2,3,4-tetramethylpentane, 2,2,4,4-tetramethylpentane, 2,3,3,4-tetramethylpentane, 2,2-dimethyl-3-ethylpentane ,
2,3-dimethyl-3-ethylpentane, 2,4
-dimethyl-3-ethylpentane, n-decane,
2,2,4,4-tetramethylhexane, 2,
2,5-trimethylheptane, 2,2,4,5-
Tetramethylhexane, 2,2,6-trimethylheptane, 2,2,3,5-tetramethylhexane, 2,2-dimethyl-4-ethylhexane,
2,2,4-trimethylheptane, 2,4-dimethyloctane, 2,4,4-trimethylheptane, 2,5,5-trimethylheptane, 2,2,
3,5-tetramethylhexane, 2,2,3,4
-tetramethylhexane, 2,2-dimethyloctane, 2,3,6-trimethylheptane, 3,
3,5-trimethylheptane, 2,4-dimethyl-3-isopropylpentane, 2,3,5-trimethylheptane, 2,4,5-trimethylheptane, 2,5-dimethyl-3-ethylhexane,
2,2,4-trimethyl-3-ethylpentane,
2,5-dimethyloctane, 2,2,3-trimethylheptane, 2,4-dimethyl-4-ethylhexane, 2,6-dimethyloctane, 2,2-dimethyl-3-ethylhexane, 2,2,3 ,4,
4-pentamethylpentane, 2-methyl-5-ethylheptane, 2,7-dimethyloctane, 3,
5-dimethyloctane, 3,6-dimethyloctane, 4-isopropylheptane, 2-methyl-4
-ethylheptane, 2,3,3-trimethylheptane, 2,2,3,3-tetramethylhexane,
4,4-dimethyloctane, 3-methyl-5-ethylheptane, 2,3,4,5-tetramethylhexane, 3,3-dimethyloctane, 4,5-dimethyloctane, 4-propylheptane, 3,4
-diethylhexane, 2,3,4-trimethylheptane, 2-methyl-3-isopropylhexane, 2,3,4,4-tetramethylhexane,
2,3-dimethyloctane, 3-methyl-3-ethylheptane, 3,3,4-trimethylheptane, 3,4,4-trimethylheptane, 3,4,
5-trimethylheptane, 2,3-dimethyl-4
-ethylhexane, 2,4-dimethyl-3-ethylhexane, 3,3-dimethyl-4-ethylhexane, 5-methylnonane, 4-methylnonane,
2,3,3,4-tetramethylhexane, 2,
2,3,3,4-pentamethylpentane, 3,4
-dimethyloctane, 2-methyl-3-ethylheptane, 3,3-diethylhexane, 2-methylnonane, 3-methyl-4-ethylheptane, 4-
Methyl-3-ethylheptane, 4-methyl-4-
Ethylheptane, 2,3,4-trimethyl-3-
Ethylpentane, 3-ethyloctane, 4-ethyloctane, 2,2,3-trimethyl-3-ethylpentane, 3-methylnonane, 2,3-dimethyl-3-ethylhexane, 3,4-dimethyl-3
Examples include -ethylhexane, 3,3,4,4-tetramethylhexane, 2-methyl-3,3-diethylpentane, n-undecane, and a mixture of two or more compounds selected from these. The content of component (c) in the whole gasoline is 1~
8% by volume, preferably 1-5% by volume. The component (d) in the present invention is an olefinic hydrocarbon having 4 to 6 carbon atoms, and specifically, for example,
1-butene, 2-butene, isobutylene, 1-pentene, 2-pentene, 2-methyl-1-butene, 3-methyl-1-butene, 2-methyl-2-
Butene, 1-hexene, 2-hexene, 3-hexene, 2-methyl-1-pentene, 3-methyl-
1-pentene, 4-methyl-1-pentene, 2-
Methyl-2-pentene, 3-methyl-2-pentene, 4-methyl-2-pentene, 2-ethyl-1
-butene, 2,3-dimethyl-1-butene, 2,
Examples include 3-dimethyl-2-butene and a mixture of two or more compounds selected from these. The content of component (d) in the total gasoline is 0 to 25% by volume, preferably 0 to 20% by volume. Component (e) in the present invention is an olefin hydrocarbon having 7 to 8 carbon atoms, and specifically, for example,
4-4-dimethyl-1-pentene, cis-4,
4, dimethyl-2-pentene, trans-4,4
-dimethyl-2-pentene, 2,3,3-trimethyl-1-butene, 2,4-dimethyl-1-pentene, 3,4-dimethyl-1-pentene, 2,4
-dimethyl-2-pentene, 3-methyl-1-hexene, 3-ethyl-1-pentene, 2,3-dimethyl-1-pentene, trans-4-methyl-
2-hexene, 5-methyl-1-hexene, trans-5-methyl-2-hexene, cis-2-methyl-3-hexene, trans-2-methyl-3
-hexene, cis-3,4-dimethyl-2-pentene, trans-3,4-dimethyl-2-pentene, 4-methyl-1-hexene, cis-4-methyl-2-hexene, 3-methyl-2 -ethyl-1
-butene, cis-5-methyl-2-hexene, 2
-Methyl-1-hexene, 1-heptene, cis-
3-Methyl-2-hexene, trans-3-methyl-2-hexene, cis-3-methyl-3-hexene, trans-3-methyl-3-hexene, 2
-ethyl-1-pentene, 3-ethyl-2-pentene, 2-methyl-2-hexene, cis-3-heptene, trans-3-heptene 2,3-dimethyl-2-pentene, trans-2-heptene, cis-2-heptene, 2,4,4-trimethyl-1
-pentene, 5,5-dimethyl-1-hexene,
Cis-2,5-dimethyl-3-hexene, trans-2,5-dimethyl-3-hexene, 3,4,
4-trimethyl-1-pentene, 3-methyl-2
-isopropyl-1-butene, 3,3-dimethyl-1-hexene, 3,5-dimethyl-1-hexene, 2,4,4-trimethyl-2-pentene,
3,3,4-trimethyl-1-pentene, cis-
2,2-dimethyl-3-hexene, trans-
2,2-dimethyl-3-hexene, cis-4,4
-dimethyl-2-hexene, trans-4,4-
Dimethyl-2-hexene, cis-5,5-dimethyl-2-hexene, trans-5,5-dimethyl-2-hexene, 4-methyl-3-ethyl-1-
Pentene, 4,4-dimethyl-1-hexene, cis-2,4-dimethyl-3-hexene, trans-2,4-dimethyl-3-hexene, 2,3,3
-trimethyl-1-pentene, 2,3,4-trimethyl-1-pentene, 4,5-dimethyl-1-
Hexene, 2,4-dimethyl-2-hexene, cis-4,5-dimethyl-2-hexene, trans-4,5-dimethyl-2-hexene, 2-methyl-3-ethyl-1-pentene, 3, 3-dimethyl-2-ethyl-1-butene, 4-methyl-2-ethyl-1-pentane, 3-ethyl-1-hexene, 2,4-dimethyl-1-hexene, 2,5-
Dimethyl-1-hexene, 3,3-dimethylhexene, cis-3,5-dimethyl-2-hexene,
3-methyl-3-ethyl-1-pentene, 3-methyl-2-ethyl-1-pentene, 6-methyl-
1-heptene, 3-ethyl-3-hexene, 2-
Examples include methyl-2-heptene, 4-octene, and a mixture of two or more compounds selected from these. The content of component (e) in the total gasoline is 0 to 7% by volume, preferably 0 to 5% by volume. Component (f) in the present invention is an olefinic hydrocarbon having 9 to 11 carbon atoms, specifically, for example,
1-nonene, cis-2-nonene, trans-2-
nonene, cis-3-nonene, trans-3-nonene, cis-4-nonene, 1-decene, 3-decene, 1-undecene, 3-undecene, trans-4-undecene, cis-5-decene, trans- Examples include 5-decene and a mixture of two or more compounds selected from these. The content of component (f) in the entire gasoline is 0 to 5% by volume, preferably 0 to 4% by volume. Component (g) in the present invention is an aromatic hydrocarbon having 6 to 7 carbon atoms, and specifically includes benzene, toluene, and mixtures thereof. The content of component (g) in the total gasoline is 3 to 8% by volume, preferably 4 to 7% by volume. Component (h) in the present invention is an aromatic hydrocarbon having 8 to 12 carbon atoms, and specifically, for example, 0-xylene, m-xylene, p-xylene, ethylbenzene, n-propylbenzene, isopropylbenzene. , 1-methyl-2-ethylbenzene, trimethylbenzene, butylbenzene, 1-methyl-
Propylbenzene, diethylbenzene, 1,2-
Dimethyl-3-ethylbenzene, 1,2,3,5
-tetramethylbenzene, 2-phenyl-3-methylbutane, 3-phenylpentane, 2-phenylpentane, 1-methyl-3-isobutylbenzene, 1-phenyl-2-methylbutane, 1,3
-dimethyl-4-isopropylbenzene, 1-ethyl-4-n-propylbenzene, n-pentylbenzene, 1-methyl-4-n-butylbenzene, 1-methyl-2,6-diethylbenzene,
1,2,4-trimethyl-5-ethylbenzene,
Examples include dimethyldiethylbenzene and a mixture of two or more compounds selected from these. The content of component (h) in the whole gasoline is
15-40% by volume, preferably 25-40% by volume. It is important that the unleaded gasoline of the present invention not only contain the above-mentioned components (a) to (h) in specific amounts, but also have a component composition that simultaneously satisfies the conditions of formulas (1) to (5). The condition for formula (1) is that the total amount of components (a) and (d) is 35
The condition of formula (2) is that the total amount of component (b), component (e) and component (g) is 15 to 30% by volume, preferably 37 to 45% by volume, and preferably 37 to 45% by volume. is 15 to 27% by volume, and the condition of formula (3) is that the total amount of component (c), component (f), and component (h) is 35 to 45% by volume, preferably 37 to 45% by volume. %. In the present invention, if the component composition of gasoline does not simultaneously satisfy the conditions of formulas (1), (2), and (3), various acceleration characteristics, low-temperature startability, and drivability (warm-up performance) may be affected. Not desirable because it is inferior. On the other hand, the condition of formula (4) is that the olefin content of the entire gasoline is 0 to 25% by volume, preferably 0 to 20% by volume.
Formula (5) also shows that the aromatic content of the entire gasoline is 50% by volume or less, preferably 45% by volume or less. In addition, the olefin content and aromatic content in formulas (5) and (6) of the present invention mean values measured by the JIS K 2536 fuel oil hydrocarbon component testing method (fluorescent indicator adsorption method). are doing. In the present invention, if the component composition of gasoline does not satisfy the conditions of equations (4) and (5), the stability of the gasoline itself may deteriorate, or the materials used in automobile exhaust gas and fuel systems may deteriorate. This is not desirable as it may have a negative effect on The blending materials used in producing the unleaded gasoline of the present invention and their blending ratios are arbitrary. light naphtha obtained by catalytic cracking, cracked gasoline obtained by catalytic cracking, hydrocracking, etc., reformed gasoline obtained by catalytic reforming, polymerized gasoline obtained by polymerization of olefins, and addition of lower olefins to hydrocarbons such as isobutane. Alkylate obtained by (alkylation), isomerate obtained by isomerization of linear lower paraffinic hydrocarbons,
De-n-
Paraffin oil, fractions thereof having a specific boiling point range, aromatic hydrocarbons, etc. can be used as the compounding material. However, in the present invention, as described above, the final blended gasoline contains specific amounts of components (a) to (h), and simultaneously satisfies the component composition conditions shown in formulas (1) to (5). It is important to satisfy the above requirements, and to achieve this, the unleaded gasoline of the present invention cannot be produced simply by mixing the above-mentioned blending materials, but rather the composition of the blending materials used and the composition of the blending materials used must be mixed. It is necessary to choose the proportions precisely. In addition, it is important that the composition of the unleaded gasoline of the present invention satisfies the above conditions, but in addition, the 10% distillation temperature specified in the fuel oil distillation test method of JIS K 2254 must be 40 to 55℃. It is desirable that the 90% distillation temperature is within the range of 150 to 175°C. Further, the unleaded gasoline of the present invention can be used as regular gasoline or high octane gasoline. When used as a regular gasoline, it should have a Research Method Octane Number of less than 95, preferably between 89 and less than 95, and when used as a high octane gasoline, it should have a Research Method Octane Number of at least 95, preferably at least 98. It is desirable that there be. The unleaded gasoline of the present invention contains the above-mentioned components (a) to (h) in specific amounts, and also contains 5 to 11 carbon atoms.
naphthenic hydrocarbons, such as cyclopentane,
Cyclohexane, methylcyclopentane, ethylcyclopentane, dimethylcyclohexane, trimethylcyclopentane, methylethylcyclopentane, dimethylcyclohexane, ethylcyclohexane, propylcyclopentane, butylcyclopentane, or a mixture of two or more compounds selected from these, etc. may contain.
Although the content of these naphthenic hydrocarbons is arbitrary, it is usually 5% by volume or less based on the total gasoline. Furthermore, in the unleaded gasoline of the present invention, if necessary, antioxidants such as phenols and amines, surface ignition inhibitors such as metal deactivators such as Schiff type compounds and thioamide type compounds, succinimide, polyalkyl Cleaning and dispersing agents such as amines and polyether amines, anti-icing agents such as polyhydric alcohols and their ethers, combustion improvers such as alkali metal and alkaline earth metal salts of organic acids, sulfuric esters of higher alcohols, anionic surfactants , cationic surfactants, amphoteric surfactants, and other antistatic agents; and azo dyes and other coloring agents. Known fuel oil additives may be added singly or in combination. Although the amount of these fuel oil additives added is arbitrary, it is usually preferable to add them so that the total amount added is 0.1% by weight or less. Furthermore, alcohols such as methanol, ethanol, isopropanol, t-butanol, and methyl-
Octane improvers such as ethers such as t-butyl ether may also be added. The amount of these octane improvers added is also optional, but it is usually 15% by weight.
The following are preferred. Examples Hereinafter, the contents of the present invention will be explained in more detail with reference to Examples and Comparative Examples. Examples and Comparative Examples 44 parts by volume of catalytically reformed gasoline obtained from Middle Eastern crude oil, 27 parts by volume of light fraction of fluidized catalytic cracked gasoline obtained from Middle Eastern crude oil, heavy fraction of catalytically reformed gasoline obtained from Middle Eastern crude oil 19 parts by volume of the fraction and 10 parts by volume of an alkylate obtained by the alkylation reaction of isobutane and lower olefin were blended to obtain the unleaded gasoline of the present invention. Table 1 shows the composition of the base material, and Table 2 shows the properties and composition of the resulting unleaded gasoline. Also, for comparison,
Table 2 shows the properties and composition of commercially available unleaded gasoline. The compositions shown in Tables 1 and 2 [excluding VO (WHOLE) and VA (WHOLE)]
All were separated, fixed, and quantified by gas chromatography/mass spectrometry (GCMS) analysis. Using the gasoline of this example and the comparative example, various performance evaluation tests were conducted as shown below, and the results were reported in the third test.
Shown in the table. [Acceleration performance test 1 (stop → low speed, low speed → medium speed, medium speed → high speed)] A passenger car (Car A) with a total displacement of 1500 c.c., manual transmission, and carburetor specification was used. Under conditions of throttle valve full throttle acceleration, shift from low gear to second gear and vehicle speed goes from 0 to 60 km/h.
hr, and the time required for the vehicle speed to reach 40 → 80 Km/hr and 80 → 120 Km/hr in top gear. [Acceleration performance test 2 (hill climbing force)] Using vehicle A, on a road with a 5% uphill slope, with the throttle valve fully open and accelerating, the vehicle speed was changed from low gear to second gear in the order of 0 to 80 km/hr, and the vehicle speed was changed to third gear. The time taken for the speed to reach from 40 to 80 km/hr was measured. [Acceleration performance test 3 (climbing power)] A passenger car (Car B) with a total displacement of 2000 c.c., an automatic transmission, and a fuel injection type was used to accelerate on an 8% uphill slope with the throttle valve fully open. The time required for the vehicle speed to reach 120 km/hr from 0 to 120 km/hr was measured in D range under the following conditions.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
発明の効果
第3表の各種性能評価試験の結果から明らかな
とおり、本発明の無鉛ガソリンは、現在市販され
ている無鉛ガソリンと比べて、停止状態から低速
への加速、低速から中速への加速、中速から高速
への加速、低速から高速への加速、登坂力などの
各種加速性能が向上するという、優れた性能を兼
ね備えたガソリンである。[Table] Effects of the Invention As is clear from the results of various performance evaluation tests shown in Table 3, the unleaded gasoline of the present invention has improved acceleration from a standstill to low speeds and from low to medium speeds compared to currently commercially available unleaded gasoline. It is a gasoline with excellent performance that improves various acceleration performance such as acceleration to high speed, acceleration from medium speed to high speed, acceleration from low speed to high speed, and hill climbing ability.
Claims (1)
〜30容量%、 (b) 炭素数7〜8のパラフイン系炭化水素10〜25
容量%、 (c) 炭素数9〜11のパラフイン系炭化水素1〜8
容量%、 (d) 炭素数4〜6のオレフイン系炭化水素0〜25
容量%、 (e) 炭素数7〜8のオレフイン系炭化水素0〜7
容量%、 (f) 炭素数9〜11のオレフイン系炭化水素0〜5
容量%、 (g) 炭素数6〜7の芳香族系炭化水素3〜8容量
%、 および (h) 炭素数8〜12の芳香族系炭化水素15〜40容量
% を必須成分として含有し、かつ以下の(1)〜(5)式の
条件を満たす成分組成を有することを特徴とする
無鉛ガソリン。 35≦(a)+(d)≦45(容量%) (1) 15≦(b)+(e)+(g)≦30(容量%) (2) 35≦(c)+(f)+(h)≦45(容量%) (3) 0≦VO(WHOLE)≦25(容量%) (4) VA(WHOLE)≦50(容量%) (5) [上式中、(a)+(d)は(a)成分および(d)成分、(b)+
(e)+(g)は(b)成分、(e)成分および(g)成分ならびに(c)
+(f)+(h)は(c)成分、(f)成分および(h)成分の合計量
(容量%)をそれぞれ示し、またVO(WHOLE)
およびVA(WHOLE)はガソリン全体のオレフ
イン分および芳香族分含量(容量%)をそれぞれ
示す。][Scope of Claims] 1 (a) Paraffinic hydrocarbon having 4 to 6 carbon atoms 15
~30% by volume, (b) 10-25 paraffinic hydrocarbons with 7-8 carbon atoms
Volume %, (c) Paraffinic hydrocarbons having 9 to 11 carbon atoms 1 to 8
Volume %, (d) Olefinic hydrocarbon having 4 to 6 carbon atoms 0 to 25
Volume %, (e) Olefinic hydrocarbon having 7 to 8 carbon atoms 0 to 7
Volume %, (f) Olefinic hydrocarbon having 9 to 11 carbon atoms 0 to 5
(g) 3 to 8 volume % of aromatic hydrocarbons having 6 to 7 carbon atoms, and (h) 15 to 40 volume % of aromatic hydrocarbons having 8 to 12 carbon atoms as essential components; An unleaded gasoline characterized by having a component composition that satisfies the conditions of formulas (1) to (5) below. 35≦(a)+(d)≦45 (capacity%) (1) 15≦(b)+(e)+(g)≦30 (capacity%) (2) 35≦(c)+(f)+ (h)≦45 (capacity%) (3) 0≦VO (WHOLE)≦25 (capacity%) (4) VA (WHOLE)≦50 (capacity%) (5) [In the above formula, (a) + ( d) is (a) component and (d) component, (b) +
(e) + (g) is (b) component, (e) component and (g) component, and (c)
+(f)+(h) indicates the total amount (volume%) of component (c), component (f), and component (h), respectively, and VO (WHOLE)
and VA (WHOLE) indicate the olefin content and aromatic content (volume %) of the entire gasoline, respectively. ]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16296687A JPS649293A (en) | 1987-06-30 | 1987-06-30 | Clear gasoline |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16296687A JPS649293A (en) | 1987-06-30 | 1987-06-30 | Clear gasoline |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS649293A JPS649293A (en) | 1989-01-12 |
JPH0470356B2 true JPH0470356B2 (en) | 1992-11-10 |
Family
ID=15764662
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16296687A Granted JPS649293A (en) | 1987-06-30 | 1987-06-30 | Clear gasoline |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS649293A (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4658991B2 (en) * | 1993-11-30 | 2011-03-23 | 出光興産株式会社 | Method for producing fuel oil for gasoline engine |
JP4658990B2 (en) * | 1993-11-30 | 2011-03-23 | 出光興産株式会社 | Method for producing fuel oil for gasoline engine |
JP3600331B2 (en) * | 1995-10-16 | 2004-12-15 | 新日本石油株式会社 | Unleaded gasoline |
US7462207B2 (en) | 1996-11-18 | 2008-12-09 | Bp Oil International Limited | Fuel composition |
US8232437B2 (en) | 1996-11-18 | 2012-07-31 | Bp Oil International Limited | Fuel composition |
FR2771419B1 (en) * | 1997-11-25 | 1999-12-31 | Inst Francais Du Petrole | HIGH-INDEX OCTANE ESSENCES AND THEIR PRODUCTION BY A PROCESS COMBINING HYDRO-ISOMERIZATION AND SEPARATION |
GB2359094A (en) * | 2000-02-14 | 2001-08-15 | Exxonmobil Res & Eng Co | Anti-foam fuel composition |
US6565617B2 (en) * | 2000-08-24 | 2003-05-20 | Shell Oil Company | Gasoline composition |
US7270687B2 (en) | 2001-05-15 | 2007-09-18 | Sunoco, Inc. | Reduced emissions transportation fuel |
US20070215519A1 (en) * | 2004-05-26 | 2007-09-20 | Jan Lodewijk Maria Dierickx | Aliphatic gasoline component and process to prepare said gasoline component |
JP4889095B2 (en) * | 2006-01-17 | 2012-02-29 | Jx日鉱日石エネルギー株式会社 | Eco-friendly gasoline composition and method for producing the same |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6116985A (en) * | 1984-07-03 | 1986-01-24 | Nippon Oil Co Ltd | Manufacture of unleaded gasoline of high octane value |
JPS63289094A (en) * | 1987-05-20 | 1988-11-25 | Nippon Oil Co Ltd | Lead-free, high-octane gasoline |
JPH0375598A (en) * | 1989-08-18 | 1991-03-29 | Hitachi Ltd | Ventilator for nuclear reactor containment vessel |
-
1987
- 1987-06-30 JP JP16296687A patent/JPS649293A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6116985A (en) * | 1984-07-03 | 1986-01-24 | Nippon Oil Co Ltd | Manufacture of unleaded gasoline of high octane value |
JPS63289094A (en) * | 1987-05-20 | 1988-11-25 | Nippon Oil Co Ltd | Lead-free, high-octane gasoline |
JPH0375598A (en) * | 1989-08-18 | 1991-03-29 | Hitachi Ltd | Ventilator for nuclear reactor containment vessel |
Also Published As
Publication number | Publication date |
---|---|
JPS649293A (en) | 1989-01-12 |
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